Progeria
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Progeria (pro-JEER-e-uh), also known as Hutchinson-Gilford syndrome, is an extremely rare, progressive genetic disorder that causes children to age rapidly, beginning in their first two years of life. Children with progeria generally appear normal at birth. During the first year, signs and symptoms, such as slow growth and hair loss, begin to appear. Heart problems or strokes are the eventual cause of death in most children with progeria. The average life expectancy for a child with progeria is about 13 years, but some with the disease die younger and some live 20 years or longer. There's no cure for progeria, but ongoing research shows some promise for treatment.
This video in 30 seconds
This video explains progeria, also known as Hutchinson-Gilford syndrome, an extremely rare, progressive genetic disorder that causes children to age rapidly beginning in their first two years of life. It covers children generally appearing normal at birth with slow growth and hair loss appearing during the first year, heart problems or strokes as the eventual cause of death in most children as described, and ongoing research as described.
Key points
- Defines progeria (Hutchinson-Gilford syndrome) as a rare progressive genetic disorder
- Covers rapid aging beginning in the first two years of life
- Covers slow growth and hair loss appearing during the first year as described
- Covers heart problems or strokes as the eventual cause of death in most children as described
- Notes life expectancy and ongoing research as described in the source
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